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Study of RN0361in Adult Healthy Subjects and Adult Hypertriglyceridemic Subjects

Sponsored by Ikaria Bioscience Pty Ltd

Quick Self-Assessment

See if you qualify and express your interest

Preparing your pre-screening questions...

Current Status

Active, Not Recruiting

Auto-verified from ClinicalTrials.gov

Verified Dec 30, 2025

Phase

Clinical Trial

Sponsor

Ikaria Bioscience Pty Ltd

Enrollment Target

108

Start Date

Sep 2024

๐Ÿ“Š
1 of 108 participants interested
1% interest

Express Your Interest Today

Interested in learning more? Complete the form below.

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Advance Medical Science

    Contribute to groundbreaking research

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel (varies by study)

  • Help Others

    Benefit future patients

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3In-person assessment if eligible
  4. 4Begin participation

About This Study

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and immunogenicity of single doses of RN0361 in Adult healthy subjects and Adult Hypertriglyceridemic Subjects.

Who Can Participate

Inclusion Criteria

Willing to provide written informed consent before any study-specific procedures.
Comply with the study requirements and restrictions as listed in the Informed Consent Form and the protocol.
Fasting serum triglyceride levels \> 80 mg/dL and fasting LDL-C โ‰ฅ70 mg/dL at screening
Female participants must either be nonchildbearing or, if of childbearing potential, not pregnant, not breastfeeding, and using effective contraception. Male participants must use condoms and ensure their partners use contraception if they are of childbearing potential.
Participants must avoid sperm or egg donation during the study

Exclusion Criteria

History or presence of any serious or uncontrolled disease
clinically significant health concerns
Recent vaccination with live vaccines, except for influenza, or plans to receive such during the study.
Positive tests for alcohol or drugs of abuse at screening.
History of multiple drug allergies or allergic reactio

โ“ Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility during the screening process.

Study Details

๐Ÿ“‹

Study Type

INTERVENTIONAL

๐Ÿ‘ฅ

Target Enrollment

108 participants

๐ŸŽ‚

Age Range

18 Years - 70 Years

โšง

Gender

ALL

๐Ÿข

Sponsor

Ikaria Bioscience Pty Ltd

Study Locations

Choose your preferred location or select flexible during enrollment

Unknown

Tamarac

Florida

Location available
View Tamarac location page
Unknown

Versailles

Kentucky

Location available
View Versailles location page
Unknown

Dilworth

Minnesota

Location available
View Dilworth location page
Unknown

Houston

Texas

Location available
View Houston location page
Unknown

Webster

Texas

Location available
View Webster location page
Unknown

Pleasant View

Utah

Location available
View Pleasant View location page

Frequently Asked Questions

Q:What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Q:Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Q:Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Q:Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

Q:How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Still have questions? Our study coordinators are here to help.

Ready to Make a Difference?

Express your interest in this groundbreaking clinical trial

๐Ÿ”’ Secure ยท ๐Ÿฅ Expert Care

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Browse all high cholesterol clinical trials in these cities โ€” not just this study.

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Looking for High Triglycerides Treatment in Lilburn?

Join others in Georgia exploring innovative treatment options through clinical research

High Triglycerides Treatment Options in Lilburn, Georgia

If you're searching for High Triglycerides treatment in Lilburn, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Lilburn, Versailles, Dilworth and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with High Triglycerides. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Georgia
Now Enrolling
Up to 108 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for High Triglycerides?

Potential Benefits

  • โœ“Access to new treatment approaches before public availability
  • โœ“Close monitoring by experienced medical professionals
  • โœ“Study-related care provided at no cost
  • โœ“Contribute to medical research for High Triglycerides

What to Expect

  • โ†’Initial screening to determine eligibility
  • โ†’Regular check-ups and monitoring visits
  • โ†’Possible compensation for time and travel
  • โ†’You can withdraw at any time

Frequently Asked Questions About This High Triglycerides Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06471543. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.